Cure JM Foundation

Yhank you! We did it! Over $850,000 raised. 113% of goal.

Cure JM announces new Mental Health Coordinator, Suzanne Edison

Cure JM launches new resources for Mental and Emotional Health

Cure JM Foundation Impact Report 2020 Now Available Online

Upcoming Events. Webinars, virtual town halls, fundraising events and more...

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Our Mission: To find a cure and better treatments for Juvenile Myositis and improve the lives of families affected by JM.

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Learn how you can help us win the fight against JM. You can make a difference today!

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Parents, Grandparents, Patients, anyone... Become a member of Cure JM. It’s free to join and the best way to help find a cure.

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Learn about JM (including juvenile dermatomyositis and juvenile polymyositis) and how to cope with this disease. Or explore the latest Cure JM research and news.

This website is provided for educational and informational purposes only. Cure JM is not engaged in rendering medical advice or professional services and this information should not be used for diagnosing or treating a health problem. The site author and the content providers make no representation or warranties, expressed or implied. Providing links to other websites does not imply that Cure JM endorses the information or services provided on those websites. The organizations operating those websites are solely responsible for the content found on their websites.
©2004-2022 Cure JM Foundation. All rights reserved.

Cure JM Foundation: Raising Awareness, Supporting Families and Funding Research to Find a Cure for Juvenile Myositis (JM) diseases, including Juvenile Dermatomyositis (JDM) and Juvenile Polymyositis (JPM). Cure JM Foundation is a 501(c)(3) non-profit organization.

Site updated 18 January, 2022.

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Our Mission: To find a cure and better treatments for Juvenile Myositis and improve the lives of families affected by JM.

JOIN CURE JM

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